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Sponsored Test

Test Code 16035

Alnylam Act® Primary Hyperoxaluria Type 1 Sponsored Testing Program

No-charge genetic testing and counseling program

45 genes

2 - 3 weeks

Test Criteria

To be eligible for the Alnylam Act® PH1 program, patients must have a family history or suspected diagnosis of primary hyperoxaluria with one or more of the following symptoms:

Family history of primary hyperoxaluria

  • Or, adult (18 years or older) with either elevated urinary oxalate OR elevated plasma oxalate
  • Or, child (less than 18 years old) with one of the following:
    • Failure to thrive and impaired kidney function
    • Nephrolithiasis
    • Nephrocalcinosis
    • Elevated urinary oxalate OR elevated plasma oxalate
Specimen(s)

Whole Blood, Saliva, OCD-100 Buccal Swab

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